A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8669



Internal ID15535195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126857167..126891305hg38UCSC Ensembl
Outerchr9:129619446..129653584hg19UCSC Ensembl
Outerchr9:128659267..128693405hg18UCSC Ensembl
Outerchr9:126699000..126733138hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385300
hg195300
hg185300
hg175300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6719
Supporting Variants
SamplesNA12156
Known GenesZBTB34
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv8669
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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